PSU || Chem || 210 || Final || Review ||
questions || with || accurate || detailed
|| answers
E2 || Reaction || - || Correct || answer || ✔One-Step || with || no || intermediates, || Base ||
takes || off || proton || + || LG || leaves || with || double || bond || formation.
What || type || of || carbons || do || E2 || rxns || favor? || - || Correct || answer || ✔Tertiary
What || is || a || Zaitsev || product? || - || Correct || answer || ✔Double || bond || formation || on ||
more || substituted || carbon
What || is || a || Hoffman || product? || - || Correct || answer || ✔Double || bond || formation || on ||
less || substituted || carbon
When || using || a || stericallly || hindered || base || (t-BuOK, || LDA), || which || product || is ||
more || favorable? || - || Correct || answer || ✔Hoffman
When || using || Eto- || or || less || sterically || hindered || base, || which || product || is || more ||
favorable? || - || Correct || answer || ✔Zaitsev
E1 || Reaction || - || Correct || answer || ✔2 || step || process, || LG || leaves || and || forms ||
carbocation, || then || base || takes || off || proton || and || makes || double || bond
